Abbott A G, Gerbi S A
Chromosoma. 1981;83(1):19-27. doi: 10.1007/BF00286013.
In the second meiotic division of spermatogenesis in Sciara coprophila the X dyad undergoes a directed nondisjunction appearing precociously at one pole. All other chromosomes behave in a normal fashion aligning on the metaphase plate and dividing. Crouse has determined that this directed nondisjunction is governed by a region of the X centromere heterochromatin known to contain the rDNA (Crouse et al., 1977; Crouse, 1979). In order to further characterize this system we have utilized DAPI c-banding and rDNA in situ hybridization to demonstrate that the precocious chromosome (X or translocation chromosome) orients at metaphase II with its centromere end juxtaposed to the pole. Even when the controlling region is not near the centromere as in the case of translocations T1 and T32, the precocious chromosome orients with the centromere end rather than the controlling region end adjacent to the pole. These data may argue that precocious positioning is established at telophase I and maintained throughout the second meiotic division. - We have examined the hypothesis that the controlling region is transcriptionally active at metaphase II and can find no evidence for this speculation. This argues that if an RNA product is related to precocious positioning it must be synthesized earlier in spermatogenesis. - An analysis of naturally occurring tetraploid spermatocytes demonstrates that the two independent precocious chromosomes of such cells are always associated with the same pole. This datum in conjunction with the observation that tetraploid primary spermatocytes have only one monopolar spindle and not two, further supports the notion that a precocious chromosome-pole interaction may be established in meiosis I and maintained throughout meiosis II.
在粪蝇精子发生的第二次减数分裂中,X二价体经历定向不分离,过早地出现在一极。所有其他染色体行为正常,在中期板上排列并分离。克劳斯已确定,这种定向不分离受X着丝粒异染色质的一个区域控制,已知该区域含有核糖体DNA(克劳斯等人,1977年;克劳斯,1979年)。为了进一步表征这个系统,我们利用DAPI C带和核糖体DNA原位杂交来证明,早熟染色体(X染色体或易位染色体)在减数分裂中期II时定向,其着丝粒端与极并列。即使控制区域不像易位T1和T32那样靠近着丝粒,早熟染色体也是以着丝粒端而不是控制区域端靠近极的方式定向。这些数据可能表明,早熟定位在末期I时就已确立,并在整个第二次减数分裂过程中保持。——我们检验了控制区域在减数分裂中期II具有转录活性这一假设,没有找到支持这一推测的证据。这表明,如果一种RNA产物与早熟定位有关,那么它一定是在精子发生的更早阶段合成的。——对自然产生的四倍体精母细胞的分析表明,这类细胞的两条独立早熟染色体总是与同一极相关联。这一数据与四倍体初级精母细胞只有一个单极纺锤体而不是两个这一观察结果相结合,进一步支持了早熟染色体 - 极相互作用可能在减数分裂I中确立并在整个减数分裂II中保持的观点。